D7Ertd443e Antibodies

AND D7Ertd443e ELISA kits, D7Ertd443e Proteins

Many biological assays use antibodies to detect D7Ertd443e, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with D7Ertd443e in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop D7Ertd443e antibodies...

We validate the specificity of these antibodies to D7Ertd443e by testing them on tissues known to express D7Ertd443e positively and negatively. Browse below to find the D7Ertd443e antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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D7Ertd443e Infographic by Boster Bio

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D7Ertd443e Overview

Facts about (E2-independent) E3 ubiquitin-conjugating enzyme FATS.

D7Ertd443e 3D structure. Source: alphafold

(E2-independent) E3 ubiquitin-conjugating enzyme FATS (D7Ertd443e)

Tumor suppressor that's required to sustain G2/M checkpoint after DNA damage. Mediates CDKN1A/p21 protein stability in a ubiquitin-independent method.

May have a function in the assembly of primary cilia. .

Gene Information

Mouse
Gene Name:	D7Ertd443e
Uniprot:	D2J0Y4
Entrez:	71007

Family

Belongs to:

No superfamily

Alternative Names

(E2-independent) E3 ubiquitin-conjugating enzyme FATS

Molecular Weight

Mass (kDA):
71.521 kDA

Genomic Context


Mouse

Location:	7 F3\|7 78.4 cM
Sequence:	7;

Tissue Specificity

Highly expressed in testis. Weak expression found in brain, lung, heart, ovary, thymus, spleen and kidney.

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/D7Ertd443e

References

PMID: 20843368 by Zhang X., et al. FATS is a transcriptional target of p53 and associated with antitumor activity.

PMID: 20154723 by Li Z., et al. An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis.